עדיין מחפשים עבודה במנועי חיפוש? הגיע הזמן להשתדרג!
במקום לעבור לבד על אלפי מודעות, Jobify מנתחת את קורות החיים שלך ומציגה לך רק משרות שבאמת מתאימות לך.
מעל 80,000 משרות • 4,000 חדשות ביום
חינם. בלי פרסומות. בלי אותיות קטנות.
מלאה
15,000-22,000 ₪
We are looking for an excellent Design Quality Engineer to join the QA product team
Job Description:
As a Design Quality Engineer, you will be the focal point for R&D projects' new products.
You will attend R&D project routine meetings as the product QA team representative.
You will review and approve deliverables and additional documents which are required for the R&D projects according to internal SOPs and regulatory requirements.
You will participate in risk-evaluation processes related to R&D projects as the product QA representative.
Act as a manager of change controls initiated throughout the R&D products and for commercial products.
Conduct QA activities relating to data analysis and statistics, calibrations, SOP reviews and approvals, audit tasks and support of non-conformity investigations.
Job Description:
As a Design Quality Engineer, you will be the focal point for R&D projects' new products.
You will attend R&D project routine meetings as the product QA team representative.
You will review and approve deliverables and additional documents which are required for the R&D projects according to internal SOPs and regulatory requirements.
You will participate in risk-evaluation processes related to R&D projects as the product QA representative.
Act as a manager of change controls initiated throughout the R&D products and for commercial products.
Conduct QA activities relating to data analysis and statistics, calibrations, SOP reviews and approvals, audit tasks and support of non-conformity investigations.
Requirements:
Education: B.Sc. in Biomedical\Biotechnology\Chemical Engineering or equivalent
Job skills:
o 2 -5 years of experience in QA/RA, preferably with R&D projects, in a medical device or pharma manufacturing company
o Deep knowledge in working according to GMP and regulatory requirements (FDA QSR 820, ISO 13485)
o Auditor qualification - an advantage
Computer skills: Proficiency in Office products - Must
Language skills: Fluent English - Mother tongue level
Personality:
o Team player
o Excellent interpersonal relations
o Highly organized and detail oriented
o Motivated and committed
o Creative and proactive
Education: B.Sc. in Biomedical\Biotechnology\Chemical Engineering or equivalent
Job skills:
o 2 -5 years of experience in QA/RA, preferably with R&D projects, in a medical device or pharma manufacturing company
o Deep knowledge in working according to GMP and regulatory requirements (FDA QSR 820, ISO 13485)
o Auditor qualification - an advantage
Computer skills: Proficiency in Office products - Must
Language skills: Fluent English - Mother tongue level
Personality:
o Team player
o Excellent interpersonal relations
o Highly organized and detail oriented
o Motivated and committed
o Creative and proactive
This position is open to all candidates.
במקום לעבור לבד על אלפי מודעות, Jobify מנתחת את קורות החיים שלך ומציגה לך רק משרות שבאמת מתאימות לך.
מעל 80,000 משרות • 4,000 חדשות ביום
חינם. בלי פרסומות. בלי אותיות קטנות.
חיפה
ערב
12 חודשים
תעודה ממשלתית
סבסוד
